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Dystonia/Parkinsonism, Hypermanganesemia, Polycythemia, and Chronic Liver Disease

Journal article published in 2014 by K. Tuschl ORCID, Pt Clayton, Sm Gospe, Pb Mills
This paper was not found in any repository; the policy of its publisher is unknown or unclear.
This paper was not found in any repository; the policy of its publisher is unknown or unclear.

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Abstract

The disorder dystonia/parkinsonism, hypermanganesemia, polycythemia, and chronic liver disease is characterized by the following: A movement disorder resulting from manganese accumulation in the basal ganglia. Whole-blood manganese concentrations that often exceed 2000 nmol/L (normal: